NEAT1 promotes genome stability via m6A methylation-dependent regulation of CHD4.

IF 7.5 1区 生物学 Q1 CELL BIOLOGY Genes & development Pub Date : 2024-10-16 DOI:10.1101/gad.351913.124
Victoria Mamontova, Barbara Trifault, Anne-Sophie Gribling-Burrer, Patrick Bohn, Lea Boten, Pit Preckwinkel, Peter Gallant, Daniel Solvie, Carsten P Ade, Dimitrios Papadopoulos, Martin Eilers, Tony Gutschner, Redmond P Smyth, Kaspar Burger
{"title":"NEAT1 promotes genome stability via m<sup>6</sup>A methylation-dependent regulation of CHD4.","authors":"Victoria Mamontova, Barbara Trifault, Anne-Sophie Gribling-Burrer, Patrick Bohn, Lea Boten, Pit Preckwinkel, Peter Gallant, Daniel Solvie, Carsten P Ade, Dimitrios Papadopoulos, Martin Eilers, Tony Gutschner, Redmond P Smyth, Kaspar Burger","doi":"10.1101/gad.351913.124","DOIUrl":null,"url":null,"abstract":"<p><p>Long noncoding (lnc)RNAs emerge as regulators of genome stability. The nuclear-enriched abundant transcript 1 (NEAT1) is overexpressed in many tumors and is responsive to genotoxic stress. However, the mechanism that links NEAT1 to DNA damage response (DDR) is unclear. Here, we investigate the expression, modification, localization, and structure of NEAT1 in response to DNA double-strand breaks (DSBs). DNA damage increases the levels and N6-methyladenosine (m<sup>6</sup>A) marks on NEAT1, which promotes alterations in NEAT1 structure, accumulation of hypermethylated NEAT1 at promoter-associated DSBs, and DSB signaling. The depletion of NEAT1 impairs DSB focus formation and elevates DNA damage. The genome-protective role of NEAT1 is mediated by the RNA methyltransferase 3 (METTL3) and involves the release of the chromodomain helicase DNA binding protein 4 (CHD4) from NEAT1 to fine-tune histone acetylation at DSBs. Our data suggest a direct role for NEAT1 in DDR.</p>","PeriodicalId":12591,"journal":{"name":"Genes & development","volume":" ","pages":"915-930"},"PeriodicalIF":7.5000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11535147/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes & development","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1101/gad.351913.124","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Long noncoding (lnc)RNAs emerge as regulators of genome stability. The nuclear-enriched abundant transcript 1 (NEAT1) is overexpressed in many tumors and is responsive to genotoxic stress. However, the mechanism that links NEAT1 to DNA damage response (DDR) is unclear. Here, we investigate the expression, modification, localization, and structure of NEAT1 in response to DNA double-strand breaks (DSBs). DNA damage increases the levels and N6-methyladenosine (m6A) marks on NEAT1, which promotes alterations in NEAT1 structure, accumulation of hypermethylated NEAT1 at promoter-associated DSBs, and DSB signaling. The depletion of NEAT1 impairs DSB focus formation and elevates DNA damage. The genome-protective role of NEAT1 is mediated by the RNA methyltransferase 3 (METTL3) and involves the release of the chromodomain helicase DNA binding protein 4 (CHD4) from NEAT1 to fine-tune histone acetylation at DSBs. Our data suggest a direct role for NEAT1 in DDR.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
NEAT1 通过 m6A 甲基化依赖性调控 CHD4 促进基因组稳定性。
长非编码(lnc)RNA是基因组稳定性的调节因子。核富集丰富转录本 1(NEAT1)在许多肿瘤中过度表达,并对基因毒性压力有反应。然而,NEAT1与DNA损伤应答(DDR)的关联机制尚不清楚。在这里,我们研究了 NEAT1 在 DNA 双链断裂(DSB)反应中的表达、修饰、定位和结构。DNA损伤增加了NEAT1上的N6-甲基腺苷(m6A)水平和标记,从而促进了NEAT1结构的改变、高甲基化的NEAT1在启动子相关DSB处的积累以及DSB信号转导。NEAT1 的耗竭会损害 DSB 病灶的形成并加剧 DNA 损伤。NEAT1 的基因组保护作用是由 RNA 甲基转移酶 3 (METTL3) 介导的,并涉及从 NEAT1 释放染色质螺旋酶 DNA 结合蛋白 4 (CHD4) 以微调 DSB 处的组蛋白乙酰化。我们的数据表明 NEAT1 在 DDR 中发挥着直接作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Genes & development
Genes & development 生物-发育生物学
CiteScore
17.50
自引率
1.90%
发文量
71
审稿时长
3-6 weeks
期刊介绍: Genes & Development is a research journal published in association with The Genetics Society. It publishes high-quality research papers in the areas of molecular biology, molecular genetics, and related fields. The journal features various research formats including Research papers, short Research Communications, and Resource/Methodology papers. Genes & Development has gained recognition and is considered as one of the Top Five Research Journals in the field of Molecular Biology and Genetics. It has an impressive Impact Factor of 12.89. The journal is ranked #2 among Developmental Biology research journals, #5 in Genetics and Heredity, and is among the Top 20 in Cell Biology (according to ISI Journal Citation Reports®, 2021).
期刊最新文献
mTORC1, the maestro of cell metabolism and growth PROSER1 modulates DNA demethylation through dual mechanisms to prevent syndromic developmental malformations Evidence for dual roles of histone H3 lysine 4 in antagonizing Polycomb group function and promoting target gene expression Proteomic insights into circadian transcription regulation: novel E-box interactors revealed by proximity labeling BRCA1 and BRCA2: from cancer susceptibility to synthetic lethality
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1